Search

everythinglearnresearchcommunity

for

Search:↓

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

A 15-year-old boy's severe scalp condition improved significantly with adalimumab and baricitinib treatment.

Abrocitinib may effectively treat stubborn alopecia universalis.

HLD10 can include increased body hair and Mongolian spots.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Deucravacitinib helped a man regrow hair significantly.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Alopecia areata is not linked to vitamin B12 deficiency.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

Abrocitinib helped a 14-year-old girl with severe alopecia areata regrow her hair significantly.

Squaric acid dibutylester can cause severe skin reactions in people with allergies.

Zinc deficiency didn't cause visible hair changes in the patient.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Early diagnosis and intervention can prevent liver-related skin issues in calves on certain pastures.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

People with chronic hair loss may have a higher chance of Vitamin B12 deficiency.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Zinc supplementation effectively treats acrodermatitis enteropathica symptoms.

Maneb causes delayed hair follicle damage in rats.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Skin changes and high vitamin B12 levels can be early signs of cancer.

A girl with Crohn's disease developed hair loss from her medication, which improved with treatment but later returned.